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Green chemistry in drug discovery : ...
~
Richardson, Paul Fenton, (1951-)
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Green chemistry in drug discovery : = from academia to industry /
紀錄類型:
書目-語言資料,印刷品 : Monograph/item
正題名/作者:
Green chemistry in drug discovery :/ edited by Paul F. Richardson.
其他題名:
from academia to industry /
其他作者:
Richardson, Paul Fenton,
出版者:
New York, NY :Humana Press, : c2022.,
面頁冊數:
xvi, 617 p. :ill. (some col.) ;26 cm.
內容註:
Green Synthesis of Common Heterocycles -- Greener Methods for Amide Bond Synthesis -- Mitsunobu Reactions in Medicinal Chemistry and Development of Practical Modifications -- Direct Nucleophilic Substitution of Alcohols by Brosnsted or Lewis Acids Activation: An Update -- Friedel-Crafts Reactions -- Ionic Liquids: Design and Applications -- Designing Efficient Cascade Reactions in Drug Discovery -- Multicomponent Synthesis: Cohesive Integration of Green Chemistry Principles -- Direct C-H Functionalization Approaches to Pharmaceutically Relevant Molecules -- C-H Activation with Photoredox Catalysis -- In Situ Protecting Groups for Chemoselective Transformations -- Expanding the Biocatalysis Toolbox -- New Directions in Coupling Chemistry -- Flow Chemistry as an Enabling Technology for Synthetic Organic Chemistry -- Reaction Optimization: A High-Throughput Experimentation Approach -- Radiopharmaceutical Discovery with 11CO2-Fixation Methods Inspired by Green Chemistry.
標題:
Drug development - Laboratory manuals. -
ISBN:
9781071620335
Green chemistry in drug discovery : = from academia to industry /
Green chemistry in drug discovery :
from academia to industry /edited by Paul F. Richardson. - New York, NY :Humana Press,c2022. - xvi, 617 p. :ill. (some col.) ;26 cm. - Methods in pharmacology and toxicology,1940-6053. - Methods in pharmacology and toxicology,..
Includes bibliographical references and index.
Green Synthesis of Common Heterocycles -- Greener Methods for Amide Bond Synthesis -- Mitsunobu Reactions in Medicinal Chemistry and Development of Practical Modifications -- Direct Nucleophilic Substitution of Alcohols by Brosnsted or Lewis Acids Activation: An Update -- Friedel-Crafts Reactions -- Ionic Liquids: Design and Applications -- Designing Efficient Cascade Reactions in Drug Discovery -- Multicomponent Synthesis: Cohesive Integration of Green Chemistry Principles -- Direct C-H Functionalization Approaches to Pharmaceutically Relevant Molecules -- C-H Activation with Photoredox Catalysis -- In Situ Protecting Groups for Chemoselective Transformations -- Expanding the Biocatalysis Toolbox -- New Directions in Coupling Chemistry -- Flow Chemistry as an Enabling Technology for Synthetic Organic Chemistry -- Reaction Optimization: A High-Throughput Experimentation Approach -- Radiopharmaceutical Discovery with 11CO2-Fixation Methods Inspired by Green Chemistry.
This detailed book highlights several emerging areas in the implementation of green chemistry in medicinal chemistry drug discovery with a specific focus on their application to the expeditious discovery of new biologically active entities. Divided into three sections, the collection explores greener approaches to chemical transformations that are both prevalent and have been highlighted as challenging within the pharmaceutical industry, overall synthetic strategy, as well as the implementation and impact of a range of enabling technologies within medicinal chemistry. As a volume of the Methods in Pharmacology and Toxicology series, chapters provide the kind of key insight that can guide researchers toward greater success in the lab. Authoritative and practical, Green Chemistry in Drug Discovery: From Academia to Industry provides both a fundamental insight into the progress that has been made as well as some of the challenges that still exist for these techniques to be effectively implemented in the drug discovery process in a routine manner.
ISBN: 9781071620335EUR159.99 Subjects--Topical Terms:
3587659
Drug development
--Laboratory manuals.
LC Class. No.: RM301.25 / .G74 2022
Dewey Class. No.: 615.1/9
National Library of Medicine Call No.: QV 745
Green chemistry in drug discovery : = from academia to industry /
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Green Synthesis of Common Heterocycles -- Greener Methods for Amide Bond Synthesis -- Mitsunobu Reactions in Medicinal Chemistry and Development of Practical Modifications -- Direct Nucleophilic Substitution of Alcohols by Brosnsted or Lewis Acids Activation: An Update -- Friedel-Crafts Reactions -- Ionic Liquids: Design and Applications -- Designing Efficient Cascade Reactions in Drug Discovery -- Multicomponent Synthesis: Cohesive Integration of Green Chemistry Principles -- Direct C-H Functionalization Approaches to Pharmaceutically Relevant Molecules -- C-H Activation with Photoredox Catalysis -- In Situ Protecting Groups for Chemoselective Transformations -- Expanding the Biocatalysis Toolbox -- New Directions in Coupling Chemistry -- Flow Chemistry as an Enabling Technology for Synthetic Organic Chemistry -- Reaction Optimization: A High-Throughput Experimentation Approach -- Radiopharmaceutical Discovery with 11CO2-Fixation Methods Inspired by Green Chemistry.
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